Danielle Posthuma
Genetics · 2009–2022
A researcher in the Science corpus: 30 papers; trusts 4 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 710 citations into it
Whom Danielle Posthuma trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Danielle Posthuma's perspective
Ordered by how strongly the researchers Danielle Posthuma trusts endorse each paper. Same corpus, a different order for every researcher.
- FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
- The support of human genetic evidence for approved drug indications (Nature Genetics)
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- FTO Obesity Variant Circuitry and Adipocyte Browning in Humans (New England Journal of Medicine)
- Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study
- Rare chromosomal deletions and duplications increase risk of schizophrenia (Nature)
- Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study (The Lancet)
- Genome-wide polygenic score to identify a monogenic risk-equivalent for coronary disease
- Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010. (The Lancet)
- Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics (PLoS Genetics)
Their papers
- Meta-analysis of the heritability of human traits based on fifty years of twin studies (2015) — 2,080 citations
- MAGMA: Generalized Gene-Set Analysis of GWAS Data (2015) — 3,357 citations
- A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) — 1,284 citations
- SynGO: an evidence-based, expert-curated knowledgebase for the synapse (2019) — 844 citations
- Functional mapping and annotation of genetic associations with FUMA (2017) — 3,703 citations
- Integrative functional genomic analysis of human brain development and neuropsychiatric risks (2018) — 740 citations
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) — 1,140 citations
- A global overview of pleiotropy and genetic architecture in complex traits (2019) — 1,107 citations
- Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2019) — 2,006 citations
- Genome-wide association studies (2021) — 1,011 citations
- The genetic architecture of the human cerebral cortex (2020) — 777 citations
- An integrated framework for local genetic correlation analysis (2022) — 352 citations
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) — 2,226 citations
- A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2021) — 813 citations
- Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) — 994 citations
- Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
- Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways (2019) — 705 citations
- Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) — 1,654 citations
- Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations
- Identification of common genetic risk variants for autism spectrum disorder (2019) — 2,059 citations